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Relevantie van observationeel onderzoek in de klinische praktijk. Themabijeenkomst “observationeel onderzoek” 20 september 2005. Ne derlandse C oöperatieve S tudie naar de A dequaatheid van D ialyse. Presentatie. NECOSAD Mogelijkheden observationeel onderzoek; voorbeelden:
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Relevantie van observationeel onderzoek in de klinische praktijk Themabijeenkomst “observationeel onderzoek” 20 september 2005
Nederlandse Coöperatieve Studienaar de Adequaatheidvan Dialyse
Presentatie • NECOSAD • Mogelijkheden observationeel onderzoek; voorbeelden: - HD versus PD - Vroege versus late start - Dialysedosis PD • Conclusies
NECOSAD • Initiatief van de Dialyse Groep Nederland (DGN) • Eerste ideeën 1991 • 1993 - 1995 NECOSAD-1 (pilot-studie) • 1997 - 2003 NECOSAD-2 Uitgevoerd in 38 dialysecentra Gefinancierd door de Nierstichting en de Ziekenfondsraad
Raad van Toezicht Prof. dr. G. K. van der Hem Prof. dr H. A. Koomans Prof. dr. K. M. L. Leunissen Dr. R. van Leusen Projectleiding Dr. E. W. Boeschoten Dr. F. W. Dekker Prof. dr. R. T. Krediet Onderzoeksverpleegkundigen NECOSAD NECOSAD – verpleegkundigen in de centra Begeleidingscommissie Dr. A. J. Apperloo, Dr. J. N. M. Barendrecht, Dr. R. J. Birnie, Dr. M. Boekhout, Dr. W. H. Boer, Dr. E. F. H. van Bommel, Prof. Dr. H. R. Büller, F. Th. de Charro, Dr. C. J. Doorenbos, Dr. W. T. van Dorp, Dr. A. van Es, Dr. W. J. Fagel, Dr. G. W. Feith, Dr. C. F. M. Franssen, Dr. L. A. M. Frenken, Dr. J. A. C. A . van Geelen, Dr. P. G. G. Gerlag, Drs. J. P. M. C. Gorgels, Dr. W. Grave, Dr. R. M. Huisman, Dr. K. J. Jager, Dr. K. Jie, Drs. W. A.. H. Koning-Mulder, Dr. M. I. Koolen, Dr. T. K. Kremer Hovinga, Drs. A. T. J. Lavrijssen, Dr. A. W. Mulder, Dr. K. J. Parlevliet, Dr. J. L. C. M. van Saase, Drs. M. J. M. Schonk, Dr. M. M. J. Schuurmans, Prof. Dr. J. G. P. Tijssen, Dr. R. M. Valentijn, Dr. GH Vastenburg, Dr. C. A. Verburgh, Dr. V. M. C. Verstappen, Dr. H. H. Vincent, Dr. P. Vos. Organisatie NECOSAD
Doelstellingen NECOSAD • Analyse van de factoren die de uitkomst van de dialysebehandeling in Nederland bepalen • Toetsen en ontwikkelen van richtlijnen voor een optimale behandeling • Bijdragen aan de kwaliteit van de behandeling door terugkoppeling van centrumgebonden resultaten en het ontwikkelen van benchmarks
Studieopzet van NECOSAD • Prospectieve observationele multi-center cohort studie bij incidente volwassen dialysepatiënten. • Binnen dit cohort gerandomiseerde trial HD versus PD
Gegevensverzameling • 4 - 0 weken voor de start: demografie, poliklinische voorbereiding, starttherapie (+ reden), primaire nierziekte, co-morbiditeit, rookgewoonten, lengte, gewicht, RR, medicijngebruik, albumine, ureum, creatinine, GFR, kwaliteit van leven • 0, 3, 6, 12, 18…..maanden dialysemodaliteit, therapiewisselingen, registratie op wachtlijst NTx, gewicht, RR, voedingstoestand, medicijngebruik, opnames, lab., dialysedosis, rGFR, Karnofsky-index, KvL.
Ingevroren materiaal • Op elk meetmoment afname van spijtmateriaal (serum, urine en dialysaat) • Vanaf 2000 werden ook bloedmonsters voor genotypering ingevroren
Presentatie • NECOSAD • Mogelijkheden observationeel onderzoek; voorbeelden: - HD versus PD - Vroege versus late start - Dialysedosis PD • Conclusies
Survival in HD and PD • Several studies show small and opposing differences between HD and PD for survival and for quality of life • Variability - due to methodological differences such as type of statistical models, case-mix and follow-up? - or due to an absence of a true difference between HD and PD ?
Design & Aim • A randomized controlled trial (RCT) within a prospective cohort • Compare survival and quality of life between Hemodialysis and Peritoneal dialysis patients
Study design • Patients without medical, social or logistic objections were invited • Patients were educated about HD and PD • Informed consent • Patients were randomized by telephone service: HD or PD • Patients were treated according to usual local care
Study design • Primary outcome: QALY in first 2 years • QALY: quality of the time spent on dialysis • Patients evaluated their own quality with EuroQol
Best imaginable state 100 80 60 40 20 Worst imaginable state 0 EuroQol
Example: QALY-scores after 2-yrs. 80.0 55.0 † 20.6
Study design • Difference of 10 QALY-points clinical relevant • Calculated sample size: 100 patients 50 HD patients 50 PD patients
Mean (SD) QALY-scores after 2 yrs.i.t.t. HD patients: 59.1 (11.7) PD patients: 54.0 (18.9) Difference HD and PD: 5.1 (p = 0.41) Difference after adjustment: 2.1 (p = 0.63) (adjusted for: age, comorbidity, primary kidney disease)
Deceased after 5-year follow-up Years 0 1 2 3 4 5 Total HD - 1 2 2 4 - 9 (50%) PD - 1 1 1 1 1 5 (25%)
Number changed modality after 5-yr follow-up Years 0 1 2 3 4 5 Total HD - 2 0 0 0 - 2 (11%) PD - 5 1 1 0 0 7 (35%)
Conclusions from the RCT HD versus PD • In terms of QALY scores HD and PD are equivalent • Better survival on PD compared to HD over the first 5 years in i.t.t. analysis • Incident dialysis patients may benefit from starting on PD
Termorshuizen et al. Hemodialysis and peritoneal dialysis: comparison of adjusted mortality rates according to the duration of dialysis: analysis of the NECOSAD 2 study. JASN 2003;14:2851-2860 Design & Aim • Prospective cohort study of patients new on dialysis treatment • Compare mortality rates between HD and PD patients
Patient characteristics – 3 months * p<0.05 HD vs PD
Patient characteristics (cont’d) * p<0.05 HD vs PD
Multivariate analysis HD compared with PDAdjusted for: ( age, gender, comorbidity, prim kidney dis, SGA, Hb, Alb, renal Kt/v baseline)
Conclusions from the prospective cohort study • During the first 2 years lower mortality rates in PD patients < 60 yr • After 2 years tendency towards greater relative mortality rates for PD patients, especially in PD patients > 60 yr • Indication of a survival benefit of long-term PD patients after switching to HD
Significant risk factors for the decline of GFR during the 1st year on dialysis relative risk effect on index GFR (mL/min) HD vs PD 1.2 -1.5 Diastolic BP (10 mm Hg ) 1.07 -0.4 Proteinuria (g/day) 1.07 -0.5 From: Jansen MAM et al. Kidney Int, 2002
Dialysis related mechanisms responsible for the decline in rGFR(adjusted for baseline GFR, age, sex, PKD, comorbidity) ß p HD: hypotensive episodes - 0.95 0.004 PD: dehydration - 1.94 0.003 Jansen et al KI 2002;62:1042-1053
Presentatie • NECOSAD • Mogelijkheden observationeel onderzoek; voorbeelden: - HD versus PD - Vroege versus late start - Dialysedosis PD • Conclusies
NECOSAD analysisKorevaar et al Lancet 2001;358:1046-1050 • Consecutive new ESRD patients > 18 yrs in 29 dialysis centres • Exclusion of patients without predialysis care and with malignancies • GFR 0-4 weeks before start dialysis • Timely start defined according to DOQ1
Initiation guideline DOQIAm J Kidney Dis 1997 • Timely initiation 1. renal Kt/Vurea 2.0/week 2. Renal Kt/Vurea < 2.0, but BMI 20 kg/m² and nPNA 0.8/kg/day • Late initiation: all other patients
Patient characteristics at start late (n=94) timely (n=159) age (yrs) 56 57 male (%) 65 60 BMI (kg/m²) 25 25 GFR (ml/min/1.73 m³) 4.9 7.1* Kt/Vurea (per week) 1.0 1.5* % HD 40 38 * = p < 0.05
Comparison between timely and late starters • Timely starters have a 2.5 month longer survival on dialysis after 3 years, but • Timely starters begin dialysis 4.1 to 8.3 months earlier in the time course of their disease • No effect of an early start of dialysis on survival
Comparison between timely and late starters • No effect of a timely start of dialysis on survival • Effect on quality of life?
ConclusionsEarly start of dialysis • NKF-DOQI targets on the start of dialysis were not evidence based • An earlier start of chronic dialysis in patients with end-stage renal disease than currently applied in developed countries is not warranted
Presentatie • NECOSAD • Mogelijkheden observationeel onderzoek; voorbeelden: - HD versus PD - Vroege versus late start - Dialysedosis PD • Conclusies
Ademex study(Paniagua R. et al. J Am Soc Nephrol, 2002) • 965 Mexican patients with peritoneal creatinine clearance < 60 L/week/1.73 m2. • Control: 4 x 2L CAPD treated: pCCr > 60 L/week/1.73 m2. • No differences in baseline characteristics. • Minimum follow-up: 2 years.